CD74-ROS1 fusion transcripts in resected non-small cell lung carcinoma
Shun Matsuura1, Kazuya Shinmura, Takaharu Kamo
1Department of Tumor Pathology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka 431-3192, Japan.
Oncology Reports
|July 24, 2013
Summary
A rare CD74-ROS1 fusion was found in one non-small cell lung cancer (NSCLC) case, suggesting its role in pulmonary carcinogenesis. This discovery aids in understanding ROS1 fusion-positive NSCLC characteristics.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Fusion oncokinases in non-small cell lung cancer (NSCLC) are clinically significant due to their sensitivity to kinase inhibitors.
- ROS1 and RET fusion oncokinases are recently identified targets in pulmonary carcinogenesis.
Purpose of the Study:
- To investigate the prevalence and characteristics of SLC34A2-ROS1, EZR-ROS1, CD74-ROS1, and KIF5B-RET fusion transcripts in 114 NSCLC cases.
- To understand the role of these fusions in the development of lung cancer.
Main Methods:
- RT-polymerase chain reaction and sequencing were used to detect fusion transcripts.
- Immunohistochemistry was employed to assess ROS1 protein expression.
- Mutation analysis of KRAS, EGFR, BRAF, PIK3CA, and p53 genes was performed.
Main Results:
- CD74-ROS1 fusion transcripts were detected in one (0.9%) of 114 NSCLCs.
- The fusion was an in-frame alteration between CD74 exon 6 and ROS1 exon 34.
- ROS1 protein overexpression was observed in cancer tissues, and no mutations were found in common oncogenes or p53.
Conclusions:
- The CD74-ROS1 fusion is implicated in the carcinogenesis of a subset of NSCLCs.
- This finding contributes to characterizing ROS1 fusion-positive NSCLC.
- Further research into ROS1 fusion-positive NSCLC is warranted.
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